Division of Life Science, Energy Institute, Institute for the Environment , The Hong Kong University of Science and Technology , Hong Kong SAR , China.
Division of Biomedical Engineering , The Hong Kong University of Science and Technology , Hong Kong SAR , China.
J Proteome Res. 2018 Sep 7;17(9):3195-3213. doi: 10.1021/acs.jproteome.8b00320. Epub 2018 Aug 22.
An in planta chemical cross-linking-based quantitative interactomics (IPQCX-MS) workflow has been developed to investigate in vivo protein-protein interactions and alteration in protein structures in a model organism, Arabidopsis thaliana. A chemical cross-linker, azide-tag-modified disuccinimidyl pimelate (AMDSP), was directly applied onto Arabidopsis tissues. Peptides produced from protein fractions of CsCl density gradient centrifugation were dimethyl-labeled, from which the AMDSP cross-linked peptides were fractionated on chromatography, enriched, and analyzed by mass spectrometry. ECL2 and SQUA-D software were used to identify and quantitate these cross-linked peptides, respectively. These computer programs integrate peptide identification with quantitation and statistical evaluation. This workflow eventually identified 354 unique cross-linked peptides, including 61 and 293 inter- and intraprotein cross-linked peptides, respectively, demonstrating that it is able to in vivo identify hundreds of cross-linked peptides at an organismal level by overcoming the difficulties caused by multiple cellular structures and complex secondary metabolites of plants. Coimmunoprecipitation and super-resolution microscopy studies have confirmed the PHB3-PHB6 protein interaction found by IPQCX-MS. The quantitative interactomics also found hormone-induced structural changes of SBPase and other proteins. This mass-spectrometry-based interactomics will be useful in the study of in vivo protein-protein interaction networks in agricultural crops and plant-microbe interactions.
已开发出一种基于植物体内化学交联的定量相互作用组学(IPQCX-MS)工作流程,用于研究模式生物拟南芥中体内蛋白质-蛋白质相互作用和蛋白质结构的变化。将一种化学交联剂,叠氮修饰的二琥珀酰亚胺基戊二酸酯(AMDSP),直接应用于拟南芥组织。从 CsCl 密度梯度离心的蛋白质部分产生的肽被二甲基标记,其中 AMDSP 交联肽在色谱上进行分离、富集,并通过质谱分析。ECL2 和 SQUA-D 软件分别用于鉴定和定量这些交联肽。这些计算机程序将肽鉴定与定量和统计评估相结合。该工作流程最终鉴定了 354 个独特的交联肽,包括 61 个和 293 个分别的互和内蛋白交联肽,证明它能够在体内通过克服植物的多种细胞结构和复杂次生代谢物引起的困难,在生物体水平上鉴定数百个交联肽。共免疫沉淀和超分辨率显微镜研究证实了 IPQCX-MS 发现的 PHB3-PHB6 蛋白相互作用。定量相互作用组学还发现了激素诱导 SBPase 和其他蛋白质的结构变化。这种基于质谱的相互作用组学将有助于研究农业作物和植物-微生物相互作用中的体内蛋白质-蛋白质相互作用网络。